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The International Journal of Biochemistry & Cell Biology|June 28, 2017
The autoinhibitory function of D1 domain of FGFR1 goes beyond the inhibition of ligand bindingLukasz Opalinski, Martyna Szczepara, Aleksandra Sokolowska-Wedzina, et al.Scientific Reports|August 4, 2017
Antibody-induced dimerization of FGFR1 promotes receptor endocytosis independently of its kinase activityŁukasz Opaliński, Aleksandra Sokołowska-Wędzina, Martyna Szczepara, et al.Journal of Molecular Biology|February 1, 2006
The dimerization mechanism of LIS1 and its implication for proteins containing the LisH motifAgnieszka Mateja, Tomasz Cierpicki, Marcin Paduch, et al.IUBMB Life|February 4, 2016
Identification of new FGF1 binding partners-Implications for its intracellular functionJoanna Bober, Sjur Olsnes, Michal Kostas, et al.Journal of Medicinal Chemistry|March 3, 2006
Exploring the Sn binding pockets in gingipains by newly developed inhibitors: structure-based design, chemistry, and activityArkadiusz Białas, Jolanta Grembecka, Daniel Krowarsch, et al.International Journal of Nanomedicine|December 11, 2012
FGF1-gold nanoparticle conjugates targeting FGFR efficiently decrease cell viability upon NIR irradiationAnna Szlachcic, Katarzyna Pala, Malgorzata Zakrzewska, et al.Protein and Peptide Letters|December 6, 2013
Protease resistant variants of FGF1 with prolonged biological activityAgnieszka Kobielak, Małgorzata Zakrzewska, Michał Kostas, et al.Biotechnology Advances|July 15, 2023
Multivalent protein-drug conjugates - An emerging strategy for the upgraded precision and efficiency of drug delivery to cancer cellsNatalia Porębska, Krzysztof Ciura, Aleksandra Chorążewska, et al.The Journal of Biological Chemistry|July 4, 2009
Increased protein stability of FGF1 can compensate for its reduced affinity for heparinMalgorzata Zakrzewska, Antoni Wiedlocha, Anna Szlachcic, et al.Biotechnology Advances|May 2, 2013
Aptamers: molecules of great potentialFilip Radom, Przemysław M Jurek, Maciej P Mazurek, et al.Pageof 12